1 Voltijd gmp jobs in Rotterdam, Nederland.

... qualification, operation and retirement. - Lead the development and implementation of site CSV strategies and governance models to ensure the ongoing validated state of GMP computerized systems throughout their lifecycle. - Partner with Automation, Engineering, Quality and Tech@Lilly teams to ensure GMP compliance, data integrity ...

... the highest quality and compliance standards. As a QA Specialist / Officer II, you will work closely with manufacturing and cross-functional teams to support GMP operations, review quality documentation, and help drive continuous improvement across our production processes. This is a fully site-based role. Working together ...

... production planning for and communicate this with relevant departments (QC/QA/Logistics and Purchase) - Ensure manufacturing activities are performed in according with GMP/quality level within the IMP department - You will be responsible for the stock levels of the department - Review and approve GMP documentation - Support the ...

JOB DESCRIPTION Work Schedule Standard (Mon-Fri) Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards Job Description Join Thermo Fisher Scientific as an intern in our Quality Control (QC) Laboratory in Groningen. During your internship, you will gain hands-on experience in a GMP-regulated ...

... productiemedewerker sluit mooi aan. Belangrijker is dat je affiniteit hebt met een farmaceutische productieomgeving en begrijpt waarom werken volgens vaste procedures en GMP zo belangrijk is. - Je hebt VMBO of MBO werk en denkniveau; - Je hebt affiniteit met farmaceutische productie en bij voorkeur kennis van GMP; - Je hebt technisch ...

... steentje bij aan de kwaliteit van verschillende farmaceutische producten. Verder ga je aan de slag met: - Het uitvoeren van celkweek conform werkprotocollen en GMP kwaliteitsrichtlijnen - Het interpreteren van de test resultaten tegen vooraf opgestelde specificaties - Het rapporteren van resultaten - Uitzendcontract via ...

... execution of microbiology activities with colleagues, providing technical guidance to ensure work is completed and reported on time. - Write, review and approve GMP documentation, including procedures, protocols and reports, in collaboration with other departments. - Represent QC as a microbiology expert during internal and ...

... (complexe) apparatuur en prepareren van monsters - Het uitvoeren van chemische analyses zoals HPLC, TLC, Dissolutie en nat-chemische analyses - Werken volgens GMP-richtlijnen - Toetsen en (her)berekenen van analyseresultaten van collega's of resultaten die buiten specificatie zijn, evalueren en rapporteren van afwijkende ...

... and strengthening the Quality Management System (QMS) at our Geleen site. As a subject matter expert in QMS and quality event processes, you will help ensure GMP compliance, support inspection readiness, and drive continuous improvement across the site. What you will get: - An agile career and dynamic working culture. ...

... werkervaring binnen de farmaceutische industrie (P3 / senior niveau) op het gebied van apparatuur-, validatie- en kalibratiewerkzaamheden. - Diepgaande kennis van GMP (in het bijzonder EU GMP Annex 1), chemie van waterige en olieachtige oplossingen, en grondige ervaring met (steriele) filtratieprocessen en apparatuur (zoals ...